Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: KEGG:D01931 (TiO2)
11,320 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In mixed industrial effluent the presence of metal ions can retard the destruction of organic contaminants and the efficiency of recovery of the metal is reduced by the presence of the organic species. Results are presented for copper-2,4-dichlorophenoxyacetic acid (2,4-D) system in which both effects occur. An electrochemical cell alone can be used to recover copper in the pH range 1.5-4.5 but it is not capable of achieving complete disappearance of 2,4-D by anodic oxidation. A photolytic cell alone can achieve the destruction of 2,4-D at pH 3.5 but leaves copper in solution. A combined photolytic-electrochemical system using an activated carbon concentrator cathode achieves the rapid simultaneous destruction of 2,4-D and recovery of copper. Results are presented for the recovery of more than 90% copper from, and >99.9%, destruction of the organochlorine compound 2,4-D in, a solution containing 100 mg dm(-3) copper and 50 mg dm(-3) 2.4-D. The photolytic degradation of 2,4-D depends on the intensity of the UV-probe. Only 19% degradation is achieved after 8 h with the 150 W UV-probe but the corresponding value with the 400 W UV-probe is 100%. In the case of 150 W UV-probe the degradation of 2,4-D proceeds through the formation of 2,4-dichlorophenol and phenol. The concentration of these intermediates are very low in the case of 400 W UV-probe because the speed of the degradation of 2,4-D is very fast. The addition of TiO2 (1 g dm(-3)), as a semiconductor material, and H202 (1.5 g dm(-3)) as an oxidant, increases the photolytic degradation of 2,4-D.
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PMID:Simultaneous recovery of copper and degradation of 2,4-dichlorophenoxyacetic acid in aqueous systems by a combination of electrolytic and photolytic processes. 1151 11

People are encouraged to wear sunscreens because of their effectiveness at reducing the risk of skin cancer. The dermal penetration of the herbicide 2,4-D can be enhanced by commercial formulations containing chemical ultraviolet (UV) absorbers, the absorbers themselves and the insect repellent DEET. This work has been extended to determine whether commercially available sunscreens containing the physical UV absorbers titanium dioxide (TiO2) or zinc oxide (ZnO) enhance the transdermal absorption of pesticides. Hairless mouse skin was pretreated with either commercially available sunscreens or the UV absorbers themselves, dissolved in phenyl trimethicone. In vitro permeability studies were performed with the pesticides 2,4-D, paraquat, parathion or malathion. The data demonstrate that pretreatment with five of the nine sunscreens tested increased the transdermal absorption of 2,4-D (P<0.05). Transdermal studies using paraquat, parathion and malathion pretreated with a representative sunscreen all demonstrated significant penetration enhancement when compared to controls (P<0.05). Repeated 2,4-D and sunscreen applications resulted in either no change between pulses or an increase in absorption after the second pulse depending on the washing regimen. Examining penetration of individual UV absorbers formulated in phenyl trimethicone showed that that ZnO can impede 2,4-D penetration and TiO2 had no effect. Combining UV absorbers in the presence of trimethicone resulted in 'sunscreens' that could actually inhibit 2,4-D penetration. Inert ingredients therefore control the increased absorption seen in commercial sunscreen products and this enhancement can be eliminated by substituting phenyl trimethicone as the solvent. Sunscreen use must still be encouraged even with the undesirable side effect of increased penetration through the skin.
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PMID:Sunscreens containing physical UV blockers can increase transdermal absorption of pesticides. 1546 32

Zeolites HY, Hbeta and HZSM-5 with different physico-chemical properties were chosen as support for TiO2 to illustrate their adsorption, dispersion and electronic structure in photocatalysis. The extent of TiO2 loading was monitored by XRD and BET surface area measurements. The adsorption capacity of HY zeolite was found to be high and hence chosen for further modification to continue the investigation. Photodegradation kinetics were carried out with 2,4-dichlorophenoxyacetic acid (2,4-D) in aqueous solution. The extent of 2,4-D degradation on TiO2/HY loading revealed the importance of adsorption in photocatalysis. Mineralisation studies on all three zeolites with 1 wt.% TiO2 loading demonstrated the good dispersion properties of TiO2/HY. Its photocatalytic activity was found to be excellent with formulated 2,4-D. Comparison of relative photonic efficiencies demonstrated that supported photocatalysts exhibited higher activity than some of the commercial photocatalysts. The high activity of supported TiO2 is due to synergistic effects of improved adsorption of 2,4-D and efficient delocalisation of photogenerated electrons by zeolite support.
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PMID:Fine route for an efficient removal of 2,4-dichlorophenoxyacetic acid (2,4-D) by zeolite-supported TiO2. 1628 43

Environmental pollution by low concentrations of 2,4-Dichlorophenoxyacetic acid (2,4-D) is a concern these days due to ever increasingly stringent regulations. Photocatalysis with immobilized TiO2 fiber is a promising oxidation method. Laboratory experiments on photocatalytic degradation of 0.045 mmol l(-1) 2,4-D with the world's first high-strength TiO2 fiber catalyst were carried out in a continuous flow reactor in which the degradations were, in general, similar to those with high 2,4-D concentrations investigated elsewhere. Degradation and mineralization of 2,4-D were significantly enhanced with no initial pH adjustments. The rate constants for total organic carbon (TOC) without pH adjustment were about two-fold bigger than the pH adjustment cases. CO2 gas measurement and carbon mass-balance were carried out for the first time, where about 34% organic carbon converted into CO2 gas during four-hour oxidation. 2,4-Dichlorophenol (2,4-DCP), phenol, benzyl alcohol and two unknowns (RT = 2.65 and 3.78 min.) were detected as aromatic intermediates while Phenol was the new aromatic in HPLC analysis. Dechlorination efficiencies were high (> 70%) in all the cases, and more than 90% efficiencies were observed in chloride mass balance. Bigger flow rates and solution temperature fixed at 20 degrees C without pH adjustment greatly enhanced 2,4-D mineralization. These results can be an important basis in applying the treatment method for dioxin-contaminated water and wastewater.
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PMID:Photocatalytic oxidation of low concentration 2,4-D solution with new TiO2 fiber catalyst in a continuous flow reactor. 1716 13

The photocatalytic degradation of many chlorinated organic compounds by semiconductor particles, has been widely recognised as a promising method of water and wastewater treatment process. In the present work the photocatalytic transformation of 2,4-D and MCPA in aqueous solution with 2 g l(-1) suspended TiO2 is demonstrated. The formation of several intermediates has been observed. The photodegradation rate increases with increasing pH. The photocatalytic transformation of 2,4-D and MCPA over TiO2 in solution containing hydrogen peroxide has been also studied. H2O, accelerated significantly the reaction rate of 2, 4-D and MCPA. The partial inhibition by ethanol is attributed to the scavenging of OH radicals involved in the first step of the reaction. Finally, from these results, a mechanism is proposed. This photocatalytic method has good potential for application on a large scale.
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PMID:Photocatalytic degradation of 2,4-dichlorophenoxyacetic acid and 4-chloro-2-methylphenoxyacetic acid in water by using TiO2. 1720

Treatment of aromatic ring compounds, 2,4-dichlorophenoxy acetic acid (2,4-D), 2,4,5-trichloro-phenoxy acetic acid (2,4,5-T), and bisphenol A, in the artificial seawater, i.e. Allen seawater, was carried out by ozonation and titanium dioxide (TiO2) photocatalyst treatment. Each compound was degraded and varnished within 30 min by only ozonolysis at pH 9.0 and at 20 degrees C, while the TOC value of each compound decreased gradually but reached almost constant value, i.e. about 70-80% of the initial value, at even 30 min of ozonation time. Ozonolysis (30 min of ozonation time) followed by TiO2 photocatalyst treatment (50h of reaction time) was a very effective method for decreasing the TOC values of aromatic ring compounds in the artificial seawater. In consequence, TOC values of 2,4-D, 2,4,5-T, and bisphenol A could be reduced to about 28, 21, and 34% of their initial values, respectively.
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PMID:Purification of seawater contaminated with undegradable aromatic ring compounds using ozonolysis followed by titanium dioxide treatment. 1806 96

Photocatalytic ozonation (O(3)/UV/TiO2) is an emerging oxidation method for recalcitrant organic contaminants in water. However, immobilised TiO2 catalysts suffer from reduced photonic efficiency. Therefore, TiO2 catalysts with excellent mechanical and thermal properties and enhanced photonic efficiencies are sought. This paper aimed to elucidate the mineralisation of low concentration 2,4-D (45.0 microM) by O(3)/UV/TiO2 using the world's first high-strength TiO2 fibre in laboratory batch experiments. 2,4-D degradation and TOC removal followed pseudo first-order reaction kinetic. The removal rates for 2,4-D and TOC in O(3)/UV/TiO2 were 1.5 and 2.4-fold larger than the summation of the values for ozonation (O3)) and photocatalysis (UV/TiO2), respectively. O(3)/UV/TiO2 was characterised by few aromatic intermediates with low abundance, fast degradations of aliphatic intermediates and dechlorination as a major step. The significantly enhanced 2,4-D mineralisation in O(3)/UV/TiO2 was attributed to increased ozone dissolution and decomposition, and reduced electron-hole recombination resulting in large number of hydroxyl radical (*OH) formation from more than one parallel path. The discrepancies in the organic carbon mass budget were attributed to few apparently major unidentified intermediates, while chlorine mass balance was reasonably acceptable. The mineralisation efficiency of O(3)/UV/TiO2 with the TiO2 fibre can further be enhanced by optimisation of experimental design parameters. The new TiO2 fibre is very promising to overcome the problem of reduced efficiency of TiO2 catalyst in an immobilised state.
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PMID:Heterogeneous photocatalytic ozonation of 2,4-D in dilute aqueous solution with TiO2 fiber. 1865 56

More efficient oxidation methods are needed to degrade especially newly emerging recalcitrant organic contaminants at low concentrations in the water environment. Reduced photonic efficiency of immobilized TiO2 is a major challenge in TiO2-assisted advanced oxidation processes (AOP). Mineralization of 2,4-dichllorophenoxyacetic acid (2,4-D) in low aqueous solution by O3/UV/TiO2 using the world's first high-strength TiO2 fiber was investigated and compared with O3, UV/TiO2, and O3/TiO2 in laboratory batch experiments. The 2,4-D degradation and total organic carbon (TOC) removal followed pseudo first-order reaction kinetic, while their rates in O3/UV/TiO2 were respectively about 1.5 and 2.4 times larger than the summation of the values in 03 and UV/TiO2. The O3/UV/TiO2 was characterized by few aromatics with very low abundance, fast disappearance of aliphatics and more than 95% dechlorination. The discrepancies in organic carbon mass balance among the intermediates and 2,4-D were attributed mainly to few apparently major unidentified intermediates. The significantly enhanced 2,4-D mineralization in O3/UV/TiO2 was attributed to increased ozone dissolution followed by its decomposition, and reduced electron-hole recombination in presence of dissolved ozone resulting in a large number of hydroxyl radical (*OH) generation from more than one parallel path. The removal efficiencies of the systems can further be enhanced by optimizing design parameters, and O3/UV/TiO2 with the TiO2 fiber is promising to mineralize recalcitrant organic contaminants in water at low concentrations.
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PMID:A novel use of TiO2 fiber for photocatalytic ozonation of 2,4-dichlorophenoxyacetic acid in aqueous solution. 1914 23

A metallic condensing cone that concentrates microwave radiation (equivalent to an optical lens) has been developed and used as part of a system to activate a microwave discharge electrodeless lamp (MDEL) in the oxidative treatment of wastewaters by aiding the novel self-ignition of the lamp on irradiation at low microwave power levels. This approach to self-ignition can potentially lead to considerable energy savings in such treatments. System performance was examined for the ignition power of microwaves of such MDEL devices in water, whose usefulness was assessed by investigating the photolytic transformation of aqueous solutions of representatives of three classes of contaminants: chlorinated phenols, herbicides and endocrine disruptors, specifically 4-chlorophenol (4-CP), 2,4-dichlorophenoxyacetic acid (2,4-D) and 4,4'-isopropylidenediphenol (bisphenol-A; BPA), respectively, taken as model wastewaters in air-equilibrated, in oxygen-saturated and in TiO2-containing aqueous media. The results are discussed in terms of the dynamics of the photo-induced degradation processes.
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PMID:Microwave discharge electrodeless lamps (MDEL). Part IV. Novel self-ignition system incorporating metallic microwave condensing cones to activate MDELs in photochemical reactions. 1986 22

A new photocatalyst, magnetic TiO2-graphene, was designed and facilely produced by combining sol-gel and assembling processes. Taking advantages of graphene and TiO2, the catalyst exhibited strong light absorption in the visible region and high adsorption capacity to organic pollutants, resulting in almost 100% photocatalytic removal efficiency of typical herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) from water under simulated solar light irradiation, far higher than 33% on commercial P25. Toxicity assessment indicates the total decomposition of the original substrate. Furthermore, the catalyst can be rapidly recovered with highly stable photocatalytic performance. After 8 successive cycles, the removal efficiency of 2,4-D maintained 97.7%, and particularly, 99.1% 2,4-D removal efficiency came back at the ninth recycle when the catalyst was re-treated by ultrasonication. Moreover, even after being laid aside for one year the catalyst still kept the 2,4-D removal efficiency as high as 95.6%. For practical application, the photocatalytic also demonstrated high removal efficiencies of herbicide 2,4-D. The photocatalyst is a promising platform for removing herbicide pollutants from water.
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PMID:Magnetic TiO2-graphene composite as a high-performance and recyclable platform for efficient photocatalytic removal of herbicides from water. 2351 Sep 91


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